Iain McIntosh

6.0k total citations
83 papers, 4.1k citations indexed

About

Iain McIntosh is a scholar working on Genetics, Molecular Biology and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Iain McIntosh has authored 83 papers receiving a total of 4.1k indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Genetics, 19 papers in Molecular Biology and 13 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Iain McIntosh's work include Cleft Lip and Palate Research (14 papers), Travel-related health issues (11 papers) and Craniofacial Disorders and Treatments (10 papers). Iain McIntosh is often cited by papers focused on Cleft Lip and Palate Research (14 papers), Travel-related health issues (11 papers) and Craniofacial Disorders and Treatments (10 papers). Iain McIntosh collaborates with scholars based in United States, United Kingdom and Mexico. Iain McIntosh's co-authors include Clair A. Francomano, Harry C. Dietz, Jacqueline T. Hecht, Gary A. Bellus, Ilkka Kaitila, William A. Horton, Terri H. Beaty, Reed E. Pyeritz, Jacqueline B. Hetmanski and Timothy Hefferon and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and Nature Genetics.

In The Last Decade

Iain McIntosh

79 papers receiving 3.9k citations

Peers

Iain McIntosh
John Rogers Australia
Richard M. Pauli United States
Reijo Norio Finland
Manuel R. Gómez United States
David Ravine Australia
J. M. Connor United Kingdom
Suvimol Hill United States
Iain McIntosh
Citations per year, relative to Iain McIntosh Iain McIntosh (= 1×) peers Ilkka Kaitila

Countries citing papers authored by Iain McIntosh

Since Specialization
Citations

This map shows the geographic impact of Iain McIntosh's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Iain McIntosh with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Iain McIntosh more than expected).

Fields of papers citing papers by Iain McIntosh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Iain McIntosh. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Iain McIntosh. The network helps show where Iain McIntosh may publish in the future.

Co-authorship network of co-authors of Iain McIntosh

This figure shows the co-authorship network connecting the top 25 collaborators of Iain McIntosh. A scholar is included among the top collaborators of Iain McIntosh based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Iain McIntosh. Iain McIntosh is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Sweeney, Elizabeth, Julie Hoover‐Fong, & Iain McIntosh. (2014). Nail-Patella Syndrome. 1 indexed citations
2.
Adamson, Elizabeth, Belinda Dewar, Jayne Donaldson, et al.. (2012). Leadership in compassionate care programme: final report.. Edinburgh Napier Research Repository (Edinburgh Napier University). 21 indexed citations
3.
Lisi, Emily C., et al.. (2007). Albinism and Developmental Delay: The Need to Test for 15q11-q13 Deletion. Pediatric Neurology. 37(4). 299–302. 3 indexed citations
4.
McIntosh, Iain, Vivien Swanson, & Karen Howell. (2006). Health Professionals’ Attitudes toward Acute Diarrhea Management. Journal of Travel Medicine. 8(2). 60–65. 6 indexed citations
5.
Lin, Shin, et al.. (2005). Phenotype Severity and Genetic Variation at the Disease Locus: An Investigation of Nail Dysplasia in the Nail Patella Syndrome. Annals of Human Genetics. 69(1). 1–8. 41 indexed citations
6.
Fallin, M. Daniele, Jacqueline B. Hetmanski, Ji Wan Park, et al.. (2003). Family‐based analysis of MSX1 haplotypes for association with oral clefts. Genetic Epidemiology. 25(2). 168–175. 37 indexed citations
7.
Hamlington, Jeanette, et al.. (2001). Twenty-two novel LMX1B mutations identified in nail patella syndrome (NPS) patients. Human Mutation. 18(5). 458–458. 27 indexed citations
8.
Eyaid, Wafaa, Mark V. Clough, Kathleen M. Scott, et al.. (1998). Physical mapping of the nail patella syndrome interval at 9q34: ordering of STSs and ESTs. Human Genetics. 103(4). 525–526. 4 indexed citations
9.
Montgomery, Robert A., et al.. (1998). Multiple Molecular Mechanisms Underlying Subdiagnostic Variants of Marfan Syndrome. The American Journal of Human Genetics. 63(6). 1703–1711. 68 indexed citations
10.
McIntosh, Iain. (1998). Health Hazards and the Elderly Traveler. Journal of Travel Medicine. 5(1). 27–29. 5 indexed citations
11.
McIntosh, Iain. (1998). Motion Sickness—Questions and Answers. Journal of Travel Medicine. 5(2). 89–91. 9 indexed citations
12.
McIntosh, Iain, Kevin Power, & Jonathan M. Reed. (1996). Prevalence, Intensity, and Sex Differences in Travel Related Stressors. Journal of Travel Medicine. 3(2). 96–102. 23 indexed citations
13.
Francomano, Clair A., Iain McIntosh, & Douglas J. Wilkin. (1996). Bone dysplasias in man: molecular insights. Current Opinion in Genetics & Development. 6(3). 301–308. 37 indexed citations
14.
Bellus, Gary A., et al.. (1996). Hypochondroplasia: Molecular Analysis of the Fibroblast Growth Factor Receptor 3 Gene. Annals of the New York Academy of Sciences. 785(1). 182–187. 20 indexed citations
15.
McClain, M. Esther, et al.. (1996). A New Measure for an Important Construct: The Attachment and Object Relations Inventory. Journal of Personality Assessment. 66(3). 604–623. 28 indexed citations
16.
Bellus, Gary A., Iain McIntosh, Elizabeth A. Smith, et al.. (1995). A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia. Nature Genetics. 10(3). 357–359. 346 indexed citations
17.
18.
Piersall, Linda, Harry C. Dietz, Bryan D. Hall, et al.. (1994). Substitution of a cysteine residue in a non-calcium binding, EGF-like domain of fibrillin segregates with the Marfan syndrome in a large kindred. Human Molecular Genetics. 3(6). 1013–1014. 9 indexed citations
19.
Kirk, J M, et al.. (1992). Variation of Sweat Sodium and Chloride with Age in Cystic Fibrosis and Normal Populations: Further Investigations in Equivocal Cases. Annals of Clinical Biochemistry International Journal of Laboratory Medicine. 29(2). 145–152. 44 indexed citations
20.
McIntosh, Iain, et al.. (1990). The haplotype distribution of the ΔF508 mutation in cystic fibrosis families in Scotland. Human Genetics. 85(4). 419–420. 9 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

Explore authors with similar magnitude of impact

Rankless by CCL
2026